Structural transitions of centromeric chromatin regulate the cell cycle-dependent recruitment of CENP-N

Genes Dev. 2015 May 15;29(10):1058-73. doi: 10.1101/gad.259432.115. Epub 2015 May 5.

Abstract

Specific recognition of centromere-specific histone variant CENP-A-containing chromatin by CENP-N is an essential process in the assembly of the kinetochore complex at centromeres prior to mammalian cell division. However, the mechanisms of CENP-N recruitment to centromeres/kinetochores remain unknown. Here, we show that a CENP-A-specific RG loop (Arg80/Gly81) plays an essential and dual regulatory role in this process. The RG loop assists the formation of a compact "ladder-like" structure of CENP-A chromatin, concealing the loop and thus impairing its role in recruiting CENP-N. Upon G1/S-phase transition, however, centromeric chromatin switches from the compact to an open state, enabling the now exposed RG loop to recruit CENP-N prior to cell division. Our results provide the first insights into the mechanisms by which the recruitment of CENP-N is regulated by the structural transitions between compaction and relaxation of centromeric chromatin during the cell cycle.

Keywords: CENP-A; CENP-N; RG loop; cell cycle; chromosome congression; higher-order chromatin structure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle / physiology*
  • Cell Line
  • Cell Proliferation
  • Centromere / chemistry*
  • Centromere / metabolism*
  • Chromatin / chemistry*
  • Chromatin / metabolism
  • Chromosomal Proteins, Non-Histone / chemistry
  • Chromosomal Proteins, Non-Histone / metabolism*
  • Chromosomes / metabolism
  • HeLa Cells
  • Humans
  • Kinetochores / chemistry
  • Kinetochores / metabolism
  • Protein Binding
  • Protein Transport
  • S Phase / physiology

Substances

  • CENPN protein, human
  • Chromatin
  • Chromosomal Proteins, Non-Histone